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自闭症谱系障碍小鼠模型中的肠道炎症。

Intestinal inflammation in a murine model of autism spectrum disorders.

机构信息

Division of Pharmacology, Utrecht Institute for Pharmaceutical Sciences, Faculty of Science, Utrecht University, Universiteitsweg 99, 3584 CG Utrecht, The Netherlands.

Division of Pharmacology, Utrecht Institute for Pharmaceutical Sciences, Faculty of Science, Utrecht University, Universiteitsweg 99, 3584 CG Utrecht, The Netherlands.

出版信息

Brain Behav Immun. 2014 Mar;37:240-7. doi: 10.1016/j.bbi.2013.12.004. Epub 2013 Dec 7.

Abstract

Autism spectrum disorder (ASD) is a cluster of neurodevelopmental disorders characterized by impairments in communication, social interest and stereotypical behaviour. Dysfunction of the intestinal tract is reported in patients with ASD and implicated in the development and severity of ASD symptoms. However, more research is required to investigate the association of intestinal problems with ASD and the potential underlying mechanisms. The purpose of this study was to investigate comorbid symptoms of intestinal inflammation in a murine model of ASD induced by prenatal exposure to valproic acid (VPA). Pregnant BALB/c females were treated subcutaneously with 600 mg/kg VPA or phosphate buffered saline on gestational day 11. Offspring were housed with their mother until weaning on postnatal day 21 (P21). All pups were exposed to a social behaviour test on P28. Inflammatory correlates and activity of the serotonergic system were measured in brain and intestinal tissue. Here we demonstrate, in addition to reduced social behaviour and increased expression of neuroinflammatory markers in the brain, that VPA in utero- exposed male offspring showed epithelial cell loss and neutrophil infiltration in the intestinal tract. Furthermore, reduced levels of serotonin were not only observed the prefrontal cortex and amygdala of VPA in utero- exposed males, but also in the small intestine. Overall, we demonstrate that gender-specific inflammatory conditions are present in the small intestines of VPA in utero- exposed mice and are accompanied by a disturbed serotonergic system in the brain as well as in the intestinal tract.

摘要

自闭症谱系障碍(ASD)是一组神经发育障碍,其特征是在沟通、社交兴趣和刻板行为方面存在障碍。自闭症患者的肠道功能障碍已被报道,并与 ASD 症状的发展和严重程度有关。然而,需要更多的研究来探讨肠道问题与 ASD 的关联以及潜在的机制。本研究旨在探讨产前暴露于丙戊酸(VPA)诱导的 ASD 小鼠模型中肠道炎症的共病症状。妊娠第 11 天,BALB/c 雌性通过皮下给予 600mg/kg VPA 或磷酸盐缓冲盐水。后代与母亲一起饲养至 21 日龄(P21)断奶。所有幼鼠均于 P28 进行社会行为测试。在大脑和肠道组织中测量炎症相关性和 5-羟色胺能系统的活性。在这里,我们除了在大脑中观察到社会行为减少和神经炎症标志物表达增加外,还发现 VPA 宫内暴露的雄性后代的肠道出现上皮细胞丢失和中性粒细胞浸润。此外,不仅在 VPA 宫内暴露的雄性的前额叶皮层和杏仁核中观察到 5-羟色胺水平降低,而且在小肠中也观察到 5-羟色胺水平降低。总的来说,我们证明了 VPA 宫内暴露的小鼠的小肠中存在特定于性别的炎症状态,并且伴随着大脑和肠道中 5-羟色胺能系统的紊乱。

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